Results 151 to 160 of about 1,383,486 (355)

National survey on diagnosis and treatment of adult anaphylaxis in Japan: The learning about anaphylaxis in adolescence and adulthood (LANA) survey Part 1

open access: yesAllergology International
Background: There have been few epidemiological surveys regarding adult anaphylaxis in Japan. The aim of the study is to investigate the current condition in the diagnosis and management of adult anaphylaxis in Japan.
Naoko Inomata   +7 more
doaj   +1 more source

Airfoil large eddy breakup devices for turbulent drag reduction [PDF]

open access: yes
It was determined from the present LaRC experiments that tandem, airfoil-shaped large eddy breakup (LEBU) devices can reduce local skin friction as much as 30 percent with a recovery region extending more than 100 boundary layer thicknesses downstream ...
Anders, J. B.
core   +1 more source

Immune‐Driven Expression in Inclusion Body Myositis With T‐Cell Large Granular Lymphocytic Leukemia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives T‐cell large granular lymphocytic leukemia (T‐LGLL), reported in up to 58% of inclusion body myositis (IBM) patients, is a rare leukemia of cytotoxic or less commonly helper T cells. The range of myopathies in T‐LGLL and the impact of coexisting T‐LGLL in IBM are not well understood. Our objectives are to investigate the spectrum of
Pannathat Soontrapa   +10 more
wiley   +1 more source

Space shuttle: Heat transfer rate measurements on Convair booster (B-15B-2) at nominal Mach number of 8 [PDF]

open access: yes
Plotted and tabulated data on heat transfer from a thin-skin thermocouple are presented. The data is representative of the reentry event of the booster alone configuration.
Martindale, W. R.   +2 more
core   +1 more source

Diagnostic Utility of the ATG9A Ratio in AP‐4–Associated Hereditary Spastic Paraplegia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Adaptor protein complex 4–associated hereditary spastic paraplegia (AP‐4‐HSP), a childhood‐onset neurogenetic disorder and frequent mimic of cerebral palsy, is caused by biallelic variants in the adaptor protein complex 4 (AP‐4) subunit genes (AP4B1 [for SPG47], AP4M1 [for SPG50], AP4E1 [for SPG51], and AP4S1 [for SPG52]).
Habibah A. P. Agianda   +12 more
wiley   +1 more source

Coronavirus disease 2019 messenger RNA vaccine skin tests and serum histamine levels in allergic reactions. [PDF]

open access: yesAnn Allergy Asthma Immunol, 2022
Kohli-Pamnani A   +3 more
europepmc   +1 more source

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